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rs11915082

From SNPedia

Orientationplus
Stabilizedplus
Make rs11915082(A;A)
Make rs11915082(A;G)
Make rs11915082(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position196082268
GeneTFRC
is asnp
is mentioned by
dbSNPrs11915082
ebirs11915082
HLIrs11915082
Exacrs11915082
Varsomers11915082
Maprs11915082
PheGenIrs11915082
hapmaprs11915082
1000 genomesrs11915082
hgdprs11915082
ensemblrs11915082
gopubmedrs11915082
geneviewrs11915082
scholarrs11915082
googlers11915082
pharmgkbrs11915082
gwascentralrs11915082
openSNPrs11915082
23andMers11915082
23andMe allrs11915082
SNP Nexus

SNPshotrs11915082
SNPdbers11915082
MSV3drs11915082
GWAS Ctlgrs11915082
GMAF0.2328
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Mean corpuscular hemoglobin
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele A
P-val 8E-13
Odds Ratio 0 [0.003-0.005] pg increase


GET Evidence
rs11915082
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.20339
summary